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1.
Water Res ; 205: 117667, 2021 Oct 15.
Article in English | MEDLINE | ID: mdl-34547698

ABSTRACT

Ferrate(VI) (Fe(VI)) can oxidize individual pollutants, but the pollutant oxidation does not necessarily result in toxicity reduction. Besides, Fe(VI) resultant Fe(III) particles has previously been used to remove heavy metals, but its influence on organic matter and toxicity of wastewater is unknown. This study investigated influence of Fe(VI) on the cytotoxicity and DNA double-strand break (DSB) effects of secondary effluents from wastewater treatment plants to Chinese hamster ovary cells. Adding 5.0 mg/L Fe(VI) as Fe reduced the cytotoxicity and genotoxicity of secondary effluents by 44%-71% and 40%-59%, respectively. The toxicity reduction could be explained by the alleviation of oxidative stress in cells when they were exposed to the Fe(VI)-treated organic matter. Oxidation and coagulation accounted for 60 and 40% of the reductions in cytotoxicity and genotoxicity, demonstrating that both oxidation and coagulation processes can play important roles in reducing toxicity. Molecular weight (MW)-distribution analysis showed that the oxidation process was favored for removing ultraviolet absorbance and fluorescence intensity of organic matter, while the coagulation process removed more dissolved organic carbon (DOC), especially the DOC of fractions with MW < 500 Da. Compared with ferric chloride, the Fe(VI) resultant Fe(III) showed better coagulation performance on organic matter, cytotoxicity and genotoxicity removal, because of the different particle sizes and crystalline structures. This study highlights the benefit of using Fe(VI) in advanced treatment as Fe(VI) reduced the overall toxicity of secondary effluents.


Subject(s)
Water Pollutants, Chemical , Water Purification , Animals , CHO Cells , Cricetinae , Cricetulus , DNA , DNA Breaks, Double-Stranded , Ferric Compounds , Iron , Oxidation-Reduction , Wastewater , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/toxicity
2.
Ecotoxicol Environ Saf ; 86: 132-40, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23062468

ABSTRACT

Textile dyes and dye industrial effluents are widely known for esthetic and toxicity problems. The toxicity of three direct dyes, Direct Blending Rebine (D-BLL), Direct Blending Scarlet (D-GLN), and Direct Blending Yellow (D-3RNL), were examined by the antioxidase and lipid peroxide index. Fish (Carassius auratus) were exposed to 100mg/L test compounds or injected with 200µg/kg corresponding dyes, and then samples of liver were collected at different times (0.5, 1, 3, 5, 7, 10, 13, 17 and 22d ) for analysis of superoxide dismutase (SOD), catalase (CAT), and contents of malondialdehyde (MDA). There is an obvious difference between two poisoning conditions and results indicated injection pattern have a more sensitive response. Besides, SOD, CAT and MDA levels displayed different variation trend following the prolonged duration, implying that dye metabolism generated less toxic or more active substance. The comparison among their intensity of enzyme inhibition showed that the toxicity order is D-BLL>D-GLN>D-3RNL. Additionally, three direct dye molecules were optimized based on the quantum mechanical charge density of a solute molecule interacting with a continuum description of the solvent (SMD) of Self-consistent Reaction Field Theory (SCRF) on B3LYP/LAN2BM level and the stable configurations were obtained. Wiberg bond orders were analyzed and atom in molecule (AIM) 2000 program was employed to estimate the interaction between atoms. The possible degradation pathways and toxicities were speculated based on the computations. The calculation is consistent with the experimental results and analysis.


Subject(s)
Biological Assay , Coloring Agents/toxicity , Goldfish/physiology , Liver/drug effects , Oxidative Stress/drug effects , Toxicity Tests/methods , Water Pollutants, Chemical/toxicity , Animals , Catalase/metabolism , Enzyme Activation/drug effects , Goldfish/metabolism , Liver/enzymology , Malondialdehyde/analysis , Models, Chemical , Superoxide Dismutase/metabolism
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